Variant report

Variant	rs57182707
Chromosome Location	chr7:63928538-63928539
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 97 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs11760441	0.82[ASN][1000 genomes]
rs11760623	0.82[ASN][1000 genomes]
rs11761642	0.82[ASN][1000 genomes]
rs11763264	0.80[ASN][1000 genomes]
rs11763268	0.80[ASN][1000 genomes]
rs11764145	0.82[ASN][1000 genomes]
rs11764842	0.82[ASN][1000 genomes]
rs11765236	0.82[ASN][1000 genomes]
rs11766677	0.82[ASN][1000 genomes]
rs11768338	0.82[ASN][1000 genomes]
rs11768668	0.82[ASN][1000 genomes]
rs11768840	0.82[ASN][1000 genomes]
rs11770985	0.80[ASN][1000 genomes]
rs11772062	0.80[ASN][1000 genomes]
rs11772218	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12113093	0.82[ASN][1000 genomes]
rs12113237	0.82[ASN][1000 genomes]
rs17138886	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17146398	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17840384	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1853407	0.86[ASN][1000 genomes]
rs34764583	0.82[ASN][1000 genomes]
rs35224539	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35255833	0.81[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs56799822	0.82[ASN][1000 genomes]
rs57093212	0.82[ASN][1000 genomes]
rs57196191	0.82[ASN][1000 genomes]
rs58450777	0.82[ASN][1000 genomes]
rs58922055	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58967958	0.82[ASN][1000 genomes]
rs59015730	0.82[ASN][1000 genomes]
rs59856772	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs60118162	0.82[ASN][1000 genomes]
rs6952579	0.82[ASN][1000 genomes]
rs6954330	0.82[ASN][1000 genomes]
rs6954460	0.82[ASN][1000 genomes]
rs6954776	0.82[ASN][1000 genomes]
rs6964427	0.82[ASN][1000 genomes]
rs6976217	0.82[ASN][1000 genomes]
rs6977201	0.82[ASN][1000 genomes]
rs73125202	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73127003	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73127006	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73127029	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73127055	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73128725	0.82[ASN][1000 genomes]
rs73128743	0.82[ASN][1000 genomes]
rs73128750	0.82[ASN][1000 genomes]
rs73128756	0.82[ASN][1000 genomes]
rs73128757	0.82[ASN][1000 genomes]
rs73128759	0.82[ASN][1000 genomes]
rs73128760	0.82[ASN][1000 genomes]
rs73128768	0.82[ASN][1000 genomes]
rs73128770	0.82[ASN][1000 genomes]
rs73128772	0.82[ASN][1000 genomes]
rs73130731	0.82[ASN][1000 genomes]
rs73130733	0.82[ASN][1000 genomes]
rs73130750	0.82[ASN][1000 genomes]
rs73130757	0.82[ASN][1000 genomes]
rs73130760	0.82[ASN][1000 genomes]
rs73130769	0.82[ASN][1000 genomes]
rs73130774	0.82[ASN][1000 genomes]
rs73130775	0.82[ASN][1000 genomes]
rs73130779	0.82[ASN][1000 genomes]
rs7776933	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7776937	0.82[ASN][1000 genomes]
rs7778593	0.82[ASN][1000 genomes]
rs7785818	0.82[ASN][1000 genomes]
rs7787877	0.82[ASN][1000 genomes]
rs7793623	0.82[ASN][1000 genomes]
rs7801917	0.82[ASN][1000 genomes]
rs7802768	0.82[ASN][1000 genomes]
rs7803294	0.82[ASN][1000 genomes]
rs7806084	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7806288	0.82[ASN][1000 genomes]
rs7806747	0.82[ASN][1000 genomes]
rs9918574	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv888255	chr7:63175168-63990100	Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
2	nsv534361	chr7:63328472-63955286	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
3	nsv888259	chr7:63363001-64009193	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
4	nsv1016466	chr7:63438466-63969492	ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
5	nsv429759	chr7:63662150-64110550	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
6	nsv429760	chr7:63687850-64110550	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
7	esv2422405	chr7:63709739-64632341	Enhancers Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
8	nsv427787	chr7:63741770-64419520	Weak transcription Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
9	nsv429761	chr7:63747498-64096138	Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
10	nsv482324	chr7:63764660-63934144	ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
11	esv2764000	chr7:63766980-64275251	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
12	nsv429762	chr7:63790450-64110550	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
13	esv2755057	chr7:63819849-64345822	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
14	nsv1031703	chr7:63839601-64225952	Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
15	nsv464518	chr7:63881238-64506904	Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
16	nsv607312	chr7:63881238-64506904	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
17	nsv1017023	chr7:63891057-63937574	Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
18	nsv1019403	chr7:63913361-63962134	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
19	nsv971488	chr7:63925778-63934218	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
20	nsv981496	chr7:63926561-63931602	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs57182707	ZNF107	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:63924800-63929200	Weak transcription	Aorta	Aorta

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